NP-MRD: Showing NP-Card for (+)-24-Methylenecycloartan-3-ol (NP0080984)

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Record Information

Version

2.0

Created at

2022-04-29 01:58:31 UTC

Updated at

2022-04-29 01:58:31 UTC

NP-MRD ID

NP0080984

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-24-Methylenecycloartan-3-ol

Description

(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,6R)-7-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-6-one belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety. (+)-24-Methylenecycloartan-3-ol is found in Mangifera indica and Xanthoceras sorbifolium. Based on a literature review very few articles have been published on (1S,3R,8R,11S,12S,15R,16R)-15-[(2R,6R)-7-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-6-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203582D          

 33 37  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652304292203582D          

 33 37  0  0  1  0            999 V2000
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   -4.1771    6.1429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8633    4.8061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2877    4.2878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
  5 11  1  1  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  8 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 16 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 19 28  1  6  0  0  0
 13 29  1  1  0  0  0
 12 30  1  6  0  0  0
  8 31  1  1  0  0  0
  6 31  1  1  0  0  0
  4 32  1  0  0  0  0
  4 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0080984

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CCC(=C)[C@@H](C)CO)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@@H]4[C@]5(C[C@@]35CC[C@]12C)CCC(=O)C4(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C31H50O2/c1-20(22(3)18-32)8-9-21(2)23-12-14-29(7)25-11-10-24-27(4,5)26(33)13-15-30(24)19-31(25,30)17-16-28(23,29)6/h21-25,32H,1,8-19H2,2-7H3/t21-,22+,23-,24+,25+,28-,29+,30-,31+/m1/s1

> <INCHI_KEY>
OKILVWSNJYSCMZ-XZTCGNEDSA-N

> <FORMULA>
C31H50O2

> <MOLECULAR_WEIGHT>
454.739

> <EXACT_MASS>
454.38108085

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
56.76575270116335

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,6R)-7-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-one

> <ALOGPS_LOGP>
5.89

> <JCHEM_LOGP>
7.097417965000002

> <ALOGPS_LOGS>
-6.45

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.881773636465407

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.61911088803897

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6532002367447771

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
136.5387

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.63e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,6R)-7-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0     -10.810  12.107   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -11.840  10.963   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0     -13.347  11.283   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0     -11.364   9.498   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.858   9.178   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.828  10.322   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -9.304  11.787   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.321  10.002   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.845   8.538   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -7.876   7.393   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.382   7.713   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.339   8.217   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.309   9.362   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.784  10.826   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -6.291  11.147   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.902   8.735   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.063   7.204   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.569   6.884   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.568   9.505   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.234   8.735   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.099   9.505   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.433   8.735   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.433   7.195   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.767   9.505   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.767  11.045   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.100   8.735   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.434   9.505   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -1.568  11.045   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.164  10.392   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.244   6.971   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.797  11.467   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -12.812   8.971   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -11.737   8.004   0.000  0.00  0.00           C+0
CONECT    1    2    7                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   32   33                                             
CONECT    5    4    6   11                                                  
CONECT    6    5    7    8   31                                             
CONECT    7    6    1                                                       
CONECT    8    6    9   15   31                                             
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    5                                                       
CONECT   12    9   13   18   30                                             
CONECT   13   12   14   16   29                                             
CONECT   14   13   15                                                       
CONECT   15   14    8                                                       
CONECT   16   13   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17   12                                                       
CONECT   19   16   20   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26                                                            
CONECT   28   19                                                            
CONECT   29   13                                                            
CONECT   30   12                                                            
CONECT   31    8    6                                                       
CONECT   32    4                                                            
CONECT   33    4                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₅₀O₂

Average Mass

454.7390 Da

Monoisotopic Mass

454.38108 Da

IUPAC Name

(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,6R)-7-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-one

Traditional Name

(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,6R)-7-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-one

CAS Registry Number

Not Available

SMILES

C[C@H](CCC(=C)[C@@H](C)CO)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@@H]4[C@]5(C[C@@]35CC[C@]12C)CCC(=O)C4(C)C

InChI Identifier

InChI=1S/C31H50O2/c1-20(22(3)18-32)8-9-21(2)23-12-14-29(7)25-11-10-24-27(4,5)26(33)13-15-30(24)19-31(25,30)17-16-28(23,29)6/h21-25,32H,1,8-19H2,2-7H3/t21-,22+,23-,24+,25+,28-,29+,30-,31+/m1/s1

InChI Key

OKILVWSNJYSCMZ-XZTCGNEDSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Mangifera indica	LOTUS Database	35616633
Xanthoceras sorbifolium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cycloartanols and derivatives

Direct Parent

Cycloartanols and derivatives

Alternative Parents

Substituents

Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Cycloartane-skeleton
Triterpenoid
26-hydroxysteroid
Monohydroxy bile acid, alcohol, or derivatives
Hydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
3-oxo-5-alpha-steroid
Oxosteroid
3-oxosteroid
Fatty alcohol
Fatty acyl
Cyclic ketone
Ketone
Organic oxide
Alcohol
Organooxygen compound
Organic oxygen compound
Carbonyl group
Primary alcohol
Hydrocarbon derivative
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.89	ALOGPS
logP	7.1	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	17.62	ChemAxon
pKa (Strongest Basic)	-1.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	136.54 m³·mol⁻¹	ChemAxon
Polarizability	56.77 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162891806

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-24-Methylenecycloartan-3-ol (NP0080984)

MOL for NP0080984 ((+)-24-Methylenecycloartan-3-ol)

3D MOL for NP0080984 ((+)-24-Methylenecycloartan-3-ol)

3D SDF for NP0080984 ((+)-24-Methylenecycloartan-3-ol)

3D-SDF for NP0080984 ((+)-24-Methylenecycloartan-3-ol)

PDB for NP0080984 ((+)-24-Methylenecycloartan-3-ol)

3D PDB for NP0080984 ((+)-24-Methylenecycloartan-3-ol)

SMILES for NP0080984 ((+)-24-Methylenecycloartan-3-ol)

INCHI for NP0080984 ((+)-24-Methylenecycloartan-3-ol)

Structure for NP0080984 ((+)-24-Methylenecycloartan-3-ol)

3D Structure for NP0080984 ((+)-24-Methylenecycloartan-3-ol)